9-azanoradamantane N—oxyl compound and method for producing same, and organic oxidation catalyst and method for oxidizing alcohols using 9-azanoradamantane N—oxyl compound

Patent metadata

Field	Value
Publication number	US-9114390-B2
Application number	US-201314380794-A
Country	US
Kind code	B2
Filing date	Feb 22, 2013
Priority date	Feb 24, 2012
Publication date	Aug 25, 2015
Grant date	Aug 25, 2015

Abstract

An organocatalyst for oxidizing alcohols in which a primary alcohol is selectively oxidized in a polyol substrate having a plurality of alcohols under environmentally-friendly conditions. The organic oxidation catalyst has an oxygen atom bonded to a nitrogen atom of an azanoradamantane skeleton and at least one alkyl group at positions 1 and 5. The oxidation catalyst has higher activity than TEMPO, which is an existing oxidation catalyst, in the selective oxidation reaction of primary alcohols, and better selectivity than AZADO and 1-Me-AZADO. This DMN-AZADO can be applied to the selective oxidation reaction of primary alcohols that contributes to shortening the synthesizing process for pharmaceuticals, pharmaceutical raw materials, agricultural chemicals, cosmetics, organic materials, and other such high value-added organic compounds.

First claim

The invention claimed is:

1. A 9-azanoradamantane N-oxyl compound represented by the following formula (1):

wherein R 1 and R 2 represent hydrogen atoms or alkyl groups, and when one of R 1 and R 2 is hydrogen, the other is an alkyl group.

2. An organic oxidation catalyst that comprises the 9-azanoradamantane N-oxyl compound of claim 1 .

3. The catalyst of claim 2 , wherein the catalyst has primary alcohol selectivity.

4. A method for producing a 9-azanoradamantane N-oxyl compound represented by the formula (1),
the method producing the 9-azanoradamantane N-oxyl compound through at least a step of oxidizing an azanoradamantane compound represented by the following formula (2):

wherein R 1 and R 2 have the same definitions as described above.

5. A method for producing a 9-azanoradamantane N-oxyl compound represented by the formula (1),
the method producing the 9-azanoradamantane N-oxyl compound through at least a step of closing the ring of a hydrazonoazabicyclo[3.3.1]nonane compound of the formula (3) below and forming an azanoradamantane ring, and oxidizing the resulting azanoradamantane compound represented by the formula (2):

wherein R 1 and R 2 have the same definitions as described above; R 3 represents at least one substituent selected from the group consisting of a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a mercapto group, an amino group, a formyl group, a carboxyl group, a sulfo group, a linear or branched C 1-12 alkyl group, a C 3-12 cycloalkyl group, a (C 1-12 alkyl)oxy group, a (C 3-12 eyeloalkyl)oxy group, a (C 1-12 alkyl) thio group, a (C 3-12 cycloalkyl)thio group, a (C 1-12 alkyl)amino group, a (C 3-12 cycloalkyl)amino group, a di(C 1-6 alkyl)amino group, a di(C 3-6 cycloalkyl)amino group, a C 1-12 alkylearbonyl group, a C 3-12 cycloalkylcarbonyl group, a (C 1-12 alkyl)oxycarbonyl group, a (C 3-12 cycloalkyl)oxycarbonyl group, a (C 1-12 alkyl)thiocarbonyl group, a (C 3-12 cycloalkyl)thiocarbonyl group, a (C 1-12 alkyl)aminocarbonyl group, a (C 3-12 cycloalkyl)aminocarbonyl group, a di(C 1-6 alkyl)aminocarbonyl group, a di(C 3-6 cycloalkyl)aminocarbonyl group, a (C 1-12 alkyl)carbonyloxy group, a (C 3-12 cycloalkyl)carbonyloxy group, a (C 1-12 alkyl)carbonylthio group, a (C 3-12 cycloalkyl)carbonylthio group, a (C 1-12 alkyl)carbonylamino group, a (C 3-12 cycloalkyl)carbonylamino group, a di(C 1-12 alkylcarbonyl)amino group, a di(C 3-12 cycloalkylcarbonyl)amino group, a C 1-6 haloalkyl group, a C 3-6 halocycloalkyl group, a C 2-6 alkenyl group, a C 3-6 cycloalkenyl group, a C 2-6 haloalkenyl group, a C 3-6 halocycloalkenyl group, a C 2-6 alkynyl group, a C 2-6 haloalkynyl group, a benzyl group which may be optionally substituted with Ra, a benzyloxy group which may be optionally substituted with Ra, a benzylthio group which may be optionally substituted with Ra, a benzylamino group which may be optionally substituted with Ra, a dibenzylamino group which may be optionally substituted with Ra, a benzylcarbonyl group which may be optionally substituted with Ra, a benzyloxycarbonyl group which may be optionally substituted with Ra, a benzylthiocarbonyl group which may be optionally substituted with Ra, a benzylaminocarbonyl group which may be optionally substituted with Ra, a dibenzylaminocarbonyl group which may be optionally substituted with Ra, a benzylcarbonyloxy group which may be optionally substituted with Ra, a benzylcarbonylthio group which may be optionally substituted with Ra, a benzylcarbonylamino group which may be optionally substituted with Ra, a di(benzylcarbonyl)amino group which may be optionally substituted with Ra, an arylamino group which may be optionally substituted with Ra, an aryloxy group which may be optionally substituted with Ra, an arylthio group which may be optionally substituted with Ra, an arylamino group which may be optionally substituted with Ra, a diarylamino group which may be optionally substituted with Ra, an arylcarbonyl group which may be optionally substituted with Ra, an aryloxycarbonyl group which may be optionally substituted with Ra, an arylthiocarbonyl group which may be optionally substituted with Ra, an arylaminocarbonyl group which may be optionally substituted with Ra, a diarylaminocarbonyl group which may be optionally substituted with Ra, an arylcarbonyloxy group which may be optionally substituted with Ra, an arylcarbonylthio group which may be optionally substituted with Ra, an arylcarbonylamino group which may be optionally substituted with Ra, and a di(arylcarbonyl)amino group which may be optionally substituted with Ra, wherein the substituents may be the same or different when two or more substituents exist; Ra represents halogen, a C 1-6 alkyl group, a C 1-6 haloalkyl group, a C 3-6 cycloalkyl group, a C 1-6 alkoxy group, a C 1-6 alkoxy C 1-6 alkyl group, a C 1-6 alkyl sulfenyl C 1-6 alkyl group, a C 1-6 haloalkoxy group, a C 1-6 alkyl sulfenyl group, a C 1-6 alkylsulfinyl group, a C 1-6 alkylsulfonyl group, a C 1-6 haloalkylsulfenyl group, a C 1-6 haloalkylsulfenyl group, a C 1-6 haloalkylsulfonyl group, a C 2-6 alkenyl group, a C 2-6 haloalkenyl group, a C 2-6 alkenyloxy group, a C 2-6 haloalkenyloxy group, a C 2-6 alkenylsulfenyl group, a C 2-6 alkenylsulfinyl group, a C 2-6 alkenylsulfonyl group, a C 2-6 haloalkenylsulfenyl group, a C 2-6 haloalkenylsulfinyl group, a C 2-6 haloalkenylsulfonyl group, a C 2-6 alkynyl group, a C 2-6 haloalkynyl group, a C 2-6 alkynyloxy group, a C 2-6 haloalkynyloxy group, a C 2-6 alkynyl sulfenyl group, a C 2-6 alkynylsulfinyl group, a C 2-6 alkynylsulfonyl group, a C 2-6 haloalkynyl sulfenyl group, a C 2-6 haloalkynylsulfinyl group, a C 2-6 haloalkynylsulfonyl group, —NO 2 , —CN, a formyl group, —OH, —SH, —NH 2 , —SCN, a C 1-6 alkoxycarbonyl group, a C 1-6 alkylcarbonyl group, a C 1-6 haloalkylcarbonyl group, a C 1-6 alkylcarbonyloxy group, a phenyl group, a C 1-6 alkylamino group, or a di C 1-6 alkylamino group, wherein Ra is substituted in numbers of 1 to 5, and may be the same or different when two or more Ra exist; and X represents a hydrogen atom, or a group selected from an acyl group, a carbamoyl group, a sulfoneamide group, an alkyl group, an allyl group, a benzyl group, an aryl group, a silyl group, a hydroxyl group, an alkoxy group, and an oxygen atom.

6. A method for producing a 9-azanoradamantane N-oxyl compound represented by the formula (1),
the method producing the 9-azanoradamantane N-oxyl compound through at least a step of condensing a keto-azabicyclo[3.3.1 ]nonane compound of the formula (4) below with phenylhydrazine, closing the ring of the resulting hydrazonoazabicyclo[3.3.1]nonane of the formula (3) and forming an azanoradamantane ring, and oxidizing the resulting azanoradamantane compound represented by the formula (2):

wherein R 1 , R 2 , and X have the same definitions as described above.

7. A method for producing a azanoradamantane N-oxyl compound represented by the formula (1),
the method comprising:
synthesizing a ketobicycloamine product through condensation of 2,6-heptanedione, ammonium chloride, and acetonedicarboxylic acid, the 2,6-heptanedione being obtained by methylating a Weinreb diamide produced from glutaryl chloride;
producing a hydrazone through condensation of the ketobicycloamine product wit

Assignees

• Univ Tohoku

Inventors

• Iwabuchi Yoshiharu
• Shibuya Masatoshi
• Doi Ryusuke

Classifications

• C07D221/22 Primary

  Bridged ring systems · CPC title

• C07D451/14

  containing 9-azabicyclo [3.3.1] nonane ring systems, e.g. granatane, 2-aza-adamantane; Cyclic acetals thereof · CPC title

• B01J2231/70

  Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues · CPC title

• C07B63/04

  Use of additives {(anti-oxidant compositions or compositions inhibiting chemical change in general C09K15/00)} · CPC title

• B01J31/0271 Primary

  also containing elements or functional groups covered by B01J31/0201 - B01J31/0231 · CPC title